Taiwan FDA registration 909a8b019a31298b03b4b3e57be46661
"Interwa" Jerry Manual Instruments for General Surgery (Unsterilized)
TW: "英特華" 傑瑞一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·INTEGRA YORK PA, INC.·Registered Aug 01, 2011 – Aug 01, 2021CancelledRegistration details
- Analysis ID
- 909a8b019a31298b03b4b3e57be46661
- Customs Code
- DHA04401066002
Company information
- Manufacturer
- INTEGRA YORK PA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Aug 01, 2011
- Expiry Date
- Aug 01, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Interwa" Jerry Manual Instruments for General Surgery (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 909a8b019a31298b03b4b3e57be46661 and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is Huizhong Co., Ltd.
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